US4259235A - Tricyclic nitrogenous compounds having string plant growth regulating properties - Google Patents
Tricyclic nitrogenous compounds having string plant growth regulating properties Download PDFInfo
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- US4259235A US4259235A US05/941,010 US94101078A US4259235A US 4259235 A US4259235 A US 4259235A US 94101078 A US94101078 A US 94101078A US 4259235 A US4259235 A US 4259235A
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/08—Bridged systems
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/44—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom three- or four-membered rings
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/62—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms three- or four-membered rings or rings with more than six members
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having alternatively specified atoms bound to the phosphorus atom and not covered by a single one of groups A01N57/10, A01N57/18, A01N57/26, A01N57/34
- A01N57/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having alternatively specified atoms bound to the phosphorus atom and not covered by a single one of groups A01N57/10, A01N57/18, A01N57/26, A01N57/34 containing heterocyclic radicals
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D205/00—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom
- C07D205/12—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D229/00—Heterocyclic compounds containing rings of less than five members having two nitrogen atoms as the only ring hetero atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/10—Spiro-condensed systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/08—Bridged systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/08—Bridged systems
Definitions
- the present invention relates to new and valuable polycyclic compounds, processes for their manufacture, crop protection agents containing these compounds, and their use as crop protection agents.
- R 3 and R 4 are individual radicals or together denote the radical (B) n ,
- A denotes the radicals --N ⁇ N--, ##STR3##
- B denotes 1 or 3 hetero atoms (O, N, S) or carbon atoms, viz., the radicals ##STR4##
- B may also, when A is ##STR5## denote the radicals ##STR6##
- n is one of the integers 0 and 1
- R 1 to R 27 are identical or different and each denotes hydrogen, or alkyl, alkenyl or alkynyl of 1 to 30 carbon atoms, preferably alkyl of 1 to 18 carbon atoms which may be cyclic or acyclic and linear or branched, phenyl or naphthyl, or a more highly condensed aromatic radical, a heterocyclic radical with one or several hetero atoms (O, N, S), or aralkyl, the aromatic radical if desired being replaced by
- the active ingredients according to the invention may be prepared from these known compounds as follows.
- ⁇ 1 - or ⁇ 2 -pyrazoline, ⁇ 2 -triazoline, pyrazolidine, isoxazolidine and ⁇ 2 -isoxazoline derivatives of compounds III to VII may be prepared in this manner by addition of stable 1,3-dipolar agents, e.g., diazo compounds, azides, azomethinimines and azomethine oxides, or of 1,3-dipolar agents which are prepared in known manner in situ, e.g., nitrile oxides and nitrilimines.
- 1,3-dipolar agents e.g., diazo compounds, azides, azomethinimines and azomethine oxides
- 1,3-dipolar agents which are prepared in known manner in situ, e.g., nitrile oxides and nitrilimines.
- the corresponding cyclopropane or aziridine derivatives are formed under the reaction conditions from the ⁇ 1 -pyrazolines or triazolines primarily formed, by elimination of N 2 .
- N 2 is eliminated by heating them in inert solvents at from 80° to 140° C., or, in the case of triazolines, by adding acids, e.g., trifluoroacetic acid, acetic acid or sulfuric acid, at from 20° to 80° C. (Examples 2D and 3B).
- acids e.g., trifluoroacetic acid, acetic acid or sulfuric acid
- the ⁇ 2 -triazoline or aziridine derivatives of compounds III to VII may be converted into the corresponding 1,2-aminohalogen, 1,2-aminohydroxy or 1,2-aminoacyloxy derivatives with hydrogen halides in water or inert solvents, or with aqueous sulfuric acid or carboxylic acids.
- the reaction takes place readily by mixing the components in water or inert solvents at from -20° to +30° C., or by heating the reaction mixture at 40° to 130° C.
- halogen or nitrogen compounds may be synthesized by reaction of the carbon double bond of the norbornene derivatives III to VII with halogens or halogen compounds, or nitric oxides or nitrogen-oxygen acids.
- the reactions have been extensively described in the literature with reference to acyclic and cyclic olefins (e.g., norbornene) (Houben-Weyl, 5/1b, 981 et seq., 5/3, 72, 95, 529, 762 and 813 et seq/., 5/4, 38 and 533 et seq., and 10/1, 61 et seq.,; Synthesis 1977, 462 et seq.), and may also be applied to derivatives III to VII.
- acyclic and cyclic olefins e.g., norbornene
- Houben-Weyl 5/1b, 981 et seq., 5/3, 72, 95, 529, 762 and 813 e
- halogen-nitrogen compounds NOCl, NO 2 Cl, NO 2 I, N-halocarboxylic acid or -sulfonic acid amides or imides, etc.
- halogen-sulfur compounds sulfenyl halides,
- halogen, pseudohalogen, nitric oxide and hydroxy compounds listed under 2. and 3. may be converted into numerous products in accordance with methods known in the art.
- the halogen compounds may be converted into the corresponding alkyl (aryl) ethers or thioethers, or hydroxy derivatives by substitution with alkali metal hydroxides, and alkali metal alcoholates, phenolates, thiolates or thiophenolates: ##STR13##
- nitric oxide derivatives (ON--, O 2 N--) may be converted into the oxime compounds by isomerization, and into the keto derivatives, nitroolefin compounds or their derivatives by hydrolysis, e.g., ##STR14##
- the hydroxy derivatives may be converted into the corresponding O-substituted derivatives by reaction with carboxylic acids, carboxylic or thiocarboxylic acid halides, chlorocarbonic or thiochlorocarbonic acid esters, phosphoric acid halides, phosphonic acid halides, thiophosphoric acid halides, thiophosphonic acid halides, phosgene, sulfonyl halides, sulfynyl halides, isocyanates, mustard oils, and carbamoyl or thiocarbamoyl halides by elimination of water or hydrogen halide, or by addition of the O--H group on to the C ⁇ O or C ⁇ N double bond: ##STR15##
- the mono- or di-nitric oxide compounds may be converted by hydrogenation into the corresponding mono- and diamine compounds, which in turn may be further reacted analogously to the hydroxy derivatives, as described above.
- the carbon double bond of the norbornene derivatives III to VII and/or the nitrogen double bond of the norbornene derivative V or the derivatives of V may be oxidized in known manner. Reaction with organic per-acids (Houben-Weyl, 6/3, 385 et seq., 10/2, 787 et seq.) gives the corresponding oxirane and/or azoxy derivatives, and reaction with OsO 4 or other oxidants (e.g., KMnO 4 ) gives the diol or hydroxyketone derivatives (Houben-Weyl, 4/1b, 604 et seq. and 861 et seq.).
- organic per-acids Houben-Weyl, 6/3, 385 et seq., 10/2, 787 et seq.
- OsO 4 or other oxidants e.g., KMnO 4
- the compounds oxidized with per-acids contain thiolether groups, the sulfone or sulfoxy derivatives are formed.
- the oxirane, sulfone or sulfoxy derivatives of V may be prepared from the corresponding derivatives of III in analogy to the conversion of III ⁇ V.
- the structure of the active ingredients was confirmed by nmr, infrared or mass spectroscopy, or by elemental analysis.
- the folling compounds were prepared in accordance with Example 1:
- Example 8 The compounds described in Example 8 and the table pertaining thereto may be used as starting compounds for the synthesis of active ingredients (cf. tables in Examples 1, 2, 4, 5, 6 and 7).
- the new active ingredients have a strong biological action on plants, i.e., they influence plant growth, either by reducing growth height, by changing the concentration of plant materials, or by destroying unwanted plants while leaving crop plants unaffected.
- Application may be effected for instance in the form of directly sprayable solutions, powders, suspensions, dispersions, emulsions, oil dispersions, pastes, dusts, broadcasting agents, or granules by spraying, atomizing, dusting, broadcasting or watering.
- the forms of application depend entirely on the purpose for which the agents are being used; in any case they should ensure a fine distribution of the active ingredient.
- mineral oil fractions of medium to high boiling point such as kerosene or diesel oil, further coal-tar oils, etc. and oils of vegetable or animal origin
- mineral oil fractions of medium to high boiling point such as kerosene or diesel oil, further coal-tar oils, etc. and oils of vegetable or animal origin
- aliphatic, cyclic and aromatic hydrocarbons such as benzene, toluene, xylene, paraffin, tetrahydronaphthalene, alkylated naphthalenes and their derivatives such as methanol, ethanol, propanol, butanol, chloroform, carbon tetrachloride, cyclohexanol, cyclohexanone, chlorobenzene, isophorone, etc.
- strongly polar solvents such as dimethylformamide, dimethyl sulfoxide, N-methylpyrrolidone, water, etc. are suitable.
- Aqueous formulations may be prepared from emulsion concentrates, pastes, oil dispersions or wettable powders by adding water.
- emulsions, pastes and oil dispersions the ingredients as such or dissolved in an oil or solvent may be homogenized in water by means of wetting or dispersing agents, adherents or emulsifiers.
- Concentrates which are suitable for dilution with water may be prepared from active ingredient, wetting agent, adherent, emulsifying or dispersing agent and possibly solvent or oil.
- surfactants are: alkali metal, alkaline earth metal and ammonium salts of ligninsulfonic acid, naphthalenesulfonic acids, phenolsulfonic acids, alkylaryl sulfonates, alkyl sulfates, and alkyl sulfonates, alkali metal and alkaline earth metal salts of dibutylnaphthalenesulfonic acid, lauryl ether sulfate, fatty alcohol sulfates, alkali metal and alkaline earth metal salts of fatty acids, salts of sulfated hexadecanols, heptadecanols, and octadecanols, salts of sulfated fatty alcohol glycol ethers, condensation products of sulfonated naphthalene and naphthalene derivatives with formaldehyde, condensation products of naphthalene or naphthalenesulf
- Powders, dusts and broadcasting agents may be prepared by mixing or grinding the active ingredients with a solid carrier.
- Granules e.g., coated, impregnated or homogeneous granules, may be prepared by bonding the active ingredients to solid carriers.
- solid carriers are mineral earths such as silicic acid, silica gels, silicates, talc, kaolin, Attaclay, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth, calcium sulfate, magnesium sulfate, magnesium oxide, ground plastics, fertilizers such as ammonium sulfate, ammonium phosphate, ammonium nitrate, and ureas, and vegetable products such as grain flours, bark meal, wood meal, and nutshell meal, cellulosic powders, etc.
- mineral earths such as silicic acid, silica gels, silicates, talc, kaolin, Attaclay, limestone, lime, chalk, bole, loess, clay, dolomite, diatomace
- the formulations contain from 0.1 to 95, and preferably 0.5 to 90, % by weight of active ingredient.
- compositions or individual active ingredients oils of various types, herbicides, fungicides, nematocides, insecticides, bactericides, trace elements, fertilizers, antifoams (e.g., silicones), and other growth regulators.
- the compounds according to the invention may prove advantageous to combine or mix with other growth-regulating active ingredients, e.g., ethylene-forming compounds of various chemical structures (such as phosphonic acid derivatives, silanes, ethyl hydrazines), and onium compounds (such as trimethylammonium, hydrazonium and sulfonium salts, and derivatives of morpholinium, piperidinium and pyridazinium compounds).
- growth-regulating active ingredients e.g., ethylene-forming compounds of various chemical structures (such as phosphonic acid derivatives, silanes, ethyl hydrazines), and onium compounds (such as trimethylammonium, hydrazonium and sulfonium salts, and derivatives of morpholinium, piperidinium and pyridazinium compounds).
- growth-regulating substances e.g., from the group of trifluoromethylsulfonamido-p-acetotoluidides, maleic hydrazide, abscisin derivatives, chlorinated phenoxy fatty acids having an auxin-like action, and polyhydric alcohols and fatty acid esters having a specific action on meristematic tissue.
- the application rate of the agents according to the invention may vary, and depends mainly on the type of effect desired; it is generally from 0.1 to 15 more more, but preferably from 0.2 to 6, kg of active ingredient per hectare.
- the agents according to the invention influence the growth of plant parts above and below the soil in different ways, and have, at the usual application concentrations, a low toxicity to warmbloods.
- the new agents have an effect on the physiology of plants, and may be used for various purposes.
- the different actions of these active ingredients depend in essence on the time of application, with reference to the development stage of the seed or plant, and on the concentrations employed.
- Vegetative and generative plant growth, and--in appropriate concentrations--germination are influenced by the new agents.
- the agents according to the invention may also find varied and extensive use in fruit crops, the cultivation of ornamentals and landscape gardening, including the influence of vegetation on uncultivated areas, airfields and training areas.
- the compounds may also be successfully used to influence blossoming and ripening, and in special cultivation processes.
- the new agents may also influence the concentration of important plant materials such as sugar and proteins.
- the active ingredients were poured, at two application rates, as aqueous formulations onto the final soil surface after sowing.
- the reductions in growth height caused by the treatment were determined by measuring the height of the plants at the end of the experiment after 30 days' growth, and comparing it with that of untreated plants.
- the prior art active ingredient N,N,N-trimethyl-N- ⁇ -chloromethylammonium chloride (CCC, German Printed Application DAS No. 1,294,734) was also used for comparison purposes.
- Spring wheat (Opal” variety) and spring barley (“Union” variety) were grown under greenhouse conditions in plastic dishes 11.5 cm in diameter, in a peat substrate provided with sufficient nutrients.
- the active ingredients were poured, at two application rates, as aqueous formulations onto the surface of the substrate after sowing.
- Leaf treatment was effected by spraying the plants at a growth height of 10 cm with aqueous formulations of the active ingredients at two application rates.
- test plants--spring wheat (Opal” variety), spring barley (“Union” variety) and spring rye (“Petkuser” variety)--were grown under greenhouse conditions in plastic dishes 11.5 cm in diameter, in a peat substrate provided with sufficient nutrients.
- the soil (preemergence) treatment was effected after sowing by pouring aqueous formulations of the active ingredients, at four application rates, onto the surface of the substrate.
- Leaf treatment was effected by spraying the plants at a growth height of 11 cm with aqueous formulations of the active ingredients, at three application rates.
- the shortening effect caused by the compounds was shown by measurements of the height of the plants at the end of the experiment.
- Plastic flowerpots having a volume of 300 cm 3 were filled with a sandy loam and the test plants placed therein (either as seed, as vegetatively reproduced species, or as potted plants, e.g., vines).
- the active ingredients were suspended or emulsified in water as vehicle and sprayed onto the surface of the soil immediately after sowing by means of finely distributing nozzles.
- the potted vines were treated by spraying them with the correspondingly diluted liquor.
- the agents were, as stated above, sprayed in water onto the leaves of the test plants, some liquor also falling onto the soil.
- solid active ingredients were first dissolved in dimethylformamide and then applied in a total liquor amount of 400 liters of water per hectare.
- the plants were first grown to a height of from 3 to 10 cm before being treated. With grasses, the first growth was cut, and the new growth treated 2 to 3 days after cutting.
- the temperature requirements of the plants were taken into account by placing them in cooler or warmer sections of the greenhouse. The experiments were run for from 4 to 6 weeks, during which time the plants were tended and their reaction to the various treatments was assessed.
- the application rates are given in kg/ha of active ingredient, regardless of the method of application and the amount of water used.
- a 0 to 100 scale was used for the evaluation, 0 denoting normal emergence or no damage (or no inhibition), and 100 denoting non-emergence or complete destruction of the plants.
- 20 parts by weight of compound 1 is well mixed with 3 parts by weight of the sodium salt of diisobutylnaphthalene- ⁇ -sulfonic acid, 17 parts by weight of the sodium salt of a lignin-sulfonic acid obtained from a sulfite waste liquor, and 60 parts by weight of powdered silica gel, and triturated in a hammer mill.
- a spray liquid is obtained containing 0.1% by weight of the active ingredient.
- compound 2 30 parts by weight of compound 2 is intimately mixed with a mixture consisting of 92 parts by weight of powdered silica gel and 8 parts by weight of paraffin oil which has been sprayed onto the surface of this silica gel.
- a formulation of the active ingredient is obtained having good adherence.
- compound 1 40 parts by weight of compound 1 is intimately mixed with 10 parts of the sodium salt of a phenolsulfonic acid-urea-formaldehyde condensate, 2 parts of silica gel and 48 parts of water to give a stable aqueous dispersion. Dilution in 100,000 parts by weight of water gives an aqueous dispersion containing 0.04 wt% of active ingredient.
- 20 parts of compound 1 is intimately mixed with 2 parts of the calcium salt of dodecylbenzenesulfonic acid, 8 parts of a fatty alcohol polyglycol ether, 2 parts of the sodium salt of a phenolsulfonic acid-urea-formaldehyde condensate and 68 parts of a paraffinic mineral oil.
- a stable oily dispersion is obtained.
- 20 parts by weight of compound 2 is dissolved in a mixture consisting of 80 parts by weight of xylene, 10 parts by weight of the adduct of 8 to 10 moles of ethylene oxide to 1 mole of oleic acid-N-monoethanolamide, 5 parts by weight of the calcium salt of dodecylbenzenesulfonic acid, and 5 parts by weight of the adduct of 40 moles of ethylene oxide to 1 mole of castor oil.
- aqueous dispersion is obtained containing 0.02% by weight of the active ingredient.
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- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Environmental Sciences (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Zoology (AREA)
- Pest Control & Pesticides (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Tricyclic nitrogenous compounds having strong plant growth regulating properties are disclosed. The compounds display the general formula ##STR1## wherein A is one of several nitrogen-containing radicals, R1, R2, R3 and R4 are selected from various recited aliphatic, aryl, araliphatic and heterocyclic groups. R3 and R4 may also together form one of a number of nitrogen, sulfur and oxygen containing radicals. These compounds have a variety of uses, including the reduction of plant growth height without harm to the plant.
Description
The present invention relates to new and valuable polycyclic compounds, processes for their manufacture, crop protection agents containing these compounds, and their use as crop protection agents.
We have found that compounds of the formula ##STR2## where R3 and R4 are individual radicals or together denote the radical (B)n, A denotes the radicals --N═N--, ##STR3## B denotes 1 or 3 hetero atoms (O, N, S) or carbon atoms, viz., the radicals ##STR4## B may also, when A is ##STR5## denote the radicals ##STR6## n is one of the integers 0 and 1, R1 to R27 are identical or different and each denotes hydrogen, or alkyl, alkenyl or alkynyl of 1 to 30 carbon atoms, preferably alkyl of 1 to 18 carbon atoms which may be cyclic or acyclic and linear or branched, phenyl or naphthyl, or a more highly condensed aromatic radical, a heterocyclic radical with one or several hetero atoms (O, N, S), or aralkyl, the aromatic radical if desired being replaced by a heterocycle with the proviso that R3 and R4 are not hydrogen and do not simultaneously denote alkyl; the abovementioned radicals, apart from hydrogen, may be mono- or polysubstituted by halogen (F, Cl, Br, I), pseudo-halogen (e.g., CN, OCN, N3, SCN), --OH, --SH, --NO2, ##STR7## (Alk,Ar)2 N--SO2 --, Alk(Ar)--N═N--, primary, secondary or tertiary alkyl, haloalkyl, haloalkoxy, haloalkylmercapto or the radicals ##STR8## Alk denoting alkyl and Ar an aromatic radical which may also be substituted as given above, further, R1 to R7 are identical or different and each denotes halogen (F, Cl, Br, I) or pseudohalogen (CN, SCN, OCN, N3), --OH ##STR9## (Alk,Ar)2 N--SO2 --, Alk(Ar)--N═N-- and further, R1 and R3 together, or R2 and R4 together, denote ═O, ═S, ═NH, ═NAlk(Ar), ═N--OH, ═N--OAlk(Ar), ═C(H,Alk,Ar)2, ##STR10## or ═N--N(H,Alk,Ar), and the radicals R8 and R9, R11 and R12, R13 and R14, R15 and R16, R21 and R22, and R23 and R24 may be linked via bridges with one or more carbon or hetero (O, N, S) atoms, have a good herbicidal and growth-regulating action which is better than that of prior art active ingredients.
The following route to compounds III to V, with R being CH3 -- and C2 H5 --, has been disclosed: reaction of quadricyclane (I) with azodicarboxylic acid diesters (II) to give III, which is converted into IV by saponification and decarboxylation and, without isolation of IV, into the azo compound V by oxidation with CuCl2, over a CuI complex (JACS, 91, 5668, 1969). ##STR11## The compound VI is obtained by partial saponification and decarboxylation of III.
Furthermore, the compound VII is known (J. Org. Chem., 33, 370 1968). ##STR12##
The active ingredients according to the invention may be prepared from these known compounds as follows.
(1) Manufacture of the compounds described in Examples 1 to 4 and the table pertaining thereto.
Reaction of compounds III to VII with 1,3-dipolar agents.
The frequently described (Houben-Weyl, 5/1b, 1119 et seq., and literature cited there) reaction of the unsubstituted norbornene with 1,3-dipolar agents to give polycyclic five-ring systems may also be carried out with the norbornene derivatives III to VII. The corresponding Δ1 - or Δ2 -pyrazoline, Δ2 -triazoline, pyrazolidine, isoxazolidine and Δ2 -isoxazoline derivatives of compounds III to VII may be prepared in this manner by addition of stable 1,3-dipolar agents, e.g., diazo compounds, azides, azomethinimines and azomethine oxides, or of 1,3-dipolar agents which are prepared in known manner in situ, e.g., nitrile oxides and nitrilimines.
In some cases, the corresponding cyclopropane or aziridine derivatives are formed under the reaction conditions from the Δ1 -pyrazolines or triazolines primarily formed, by elimination of N2.
With the stable triazolines and Δ1 -pyrazolines, N2 is eliminated by heating them in inert solvents at from 80° to 140° C., or, in the case of triazolines, by adding acids, e.g., trifluoroacetic acid, acetic acid or sulfuric acid, at from 20° to 80° C. (Examples 2D and 3B).
The reaction of the Δ1 - or N-H-Δ2 -pyrazoline compounds with carboxylic acids, carboxylic acid or thiocarboxylic acid halides, carboxylic acid anhydrides, esters of chlorocarbonic acid and thiochlorocarbonic acid, phosgene, sulfo acids, sulfonyl halides, sulfynyl halides, sulfenyl halides, alkyl, alkenyl or alkynyl halides, aldehydes or ketones, isocyanates, mustard oils, and carbamoyl or thiocarbamoyl halides gives, as a result of the elimination of water or hydrogen halide, or as a result of the addition of the N--H group on to the C═O or C═N double bond, the corresponding N-substituted Δ2 -pyrazoline derivatives.
These reactions are carried out in accordance with well-known methods by heating the compounds, if desired in inert solvents and in the presence of auxiliary bases, e.g., tertiary amines, alkali metal carbonates or bicarbonates, sodium methylate, sodium hydride, alkali metal hydroxide, etc., at from 20° to 160° C. (Example 2B).
2. Manufacture of the compounds described in Example 5A and the table pertaining thereto.
Ring opening of the Δ2 -triazoline or aziridine derivatives of III to VII with acids.
The Δ2 -triazoline or aziridine derivatives of compounds III to VII may be converted into the corresponding 1,2-aminohalogen, 1,2-aminohydroxy or 1,2-aminoacyloxy derivatives with hydrogen halides in water or inert solvents, or with aqueous sulfuric acid or carboxylic acids. The reaction takes place readily by mixing the components in water or inert solvents at from -20° to +30° C., or by heating the reaction mixture at 40° to 130° C.
3. Manufacture of the compounds described in Examples 5B-E and the table pertaining thereto.
Reaction of compounds III to VII with halogens or halogen compounds, or nitric oxides or nitrogen-oxygen acids.
Numerous halogen or nitrogen compounds may be synthesized by reaction of the carbon double bond of the norbornene derivatives III to VII with halogens or halogen compounds, or nitric oxides or nitrogen-oxygen acids. The reactions have been extensively described in the literature with reference to acyclic and cyclic olefins (e.g., norbornene) (Houben-Weyl, 5/1b, 981 et seq., 5/3, 72, 95, 529, 762 and 813 et seq/., 5/4, 38 and 533 et seq., and 10/1, 61 et seq.,; Synthesis 1977, 462 et seq.), and may also be applied to derivatives III to VII. Thus, reaction with halogens, interhalogen compounds, hydrogen halides, hypohalides, halogen pseudohalides (azides, cyamides, cyanates, thiocyanates), halogen-nitrogen compounds (NOCl, NO2 Cl, NO2 I, N-halocarboxylic acid or -sulfonic acid amides or imides, etc.), halogen-sulfur compounds (sulfenyl halides, sulfonyl halides, etc.), nitric oxides (N2 O3, N2 O4, N2 O5) or nitrogen-oxygen acids (e.g., HNO3) gives the corresponding addition compounds (Examples 5B-D).
From some adducts of III or VII (R=SO2 Cl), the corresponding adducts of V or VII (R=H) may be prepared analogously to the conversion of III→V or VII (R=SO2 Cl)→VII (R=H), the monosubstituted norbornene derivatives also being formed to a certain extent as a result of hydrogen halide elimination (reverse formation of the carbon double bond).
The halogen, pseudohalogen, nitric oxide and hydroxy compounds listed under 2. and 3. may be converted into numerous products in accordance with methods known in the art.
Thus, for instance, the halogen compounds may be converted into the corresponding alkyl (aryl) ethers or thioethers, or hydroxy derivatives by substitution with alkali metal hydroxides, and alkali metal alcoholates, phenolates, thiolates or thiophenolates: ##STR13##
The nitric oxide derivatives (ON--, O2 N--) may be converted into the oxime compounds by isomerization, and into the keto derivatives, nitroolefin compounds or their derivatives by hydrolysis, e.g., ##STR14##
The hydroxy derivatives may be converted into the corresponding O-substituted derivatives by reaction with carboxylic acids, carboxylic or thiocarboxylic acid halides, chlorocarbonic or thiochlorocarbonic acid esters, phosphoric acid halides, phosphonic acid halides, thiophosphoric acid halides, thiophosphonic acid halides, phosgene, sulfonyl halides, sulfynyl halides, isocyanates, mustard oils, and carbamoyl or thiocarbamoyl halides by elimination of water or hydrogen halide, or by addition of the O--H group on to the C═O or C═N double bond: ##STR15##
The mono- or di-nitric oxide compounds (ON--, O2 N--, ═N--OH) may be converted by hydrogenation into the corresponding mono- and diamine compounds, which in turn may be further reacted analogously to the hydroxy derivatives, as described above.
4. Manufacture of the compounds described in Example 6 and the table pertaining thereto.
Oxidation of compounds III to VII, or derivatives prepared therefrom according to 1., 2., and 3.
The carbon double bond of the norbornene derivatives III to VII and/or the nitrogen double bond of the norbornene derivative V or the derivatives of V, which may be prepared by the methods described above (1., 2. and 3.), may be oxidized in known manner. Reaction with organic per-acids (Houben-Weyl, 6/3, 385 et seq., 10/2, 787 et seq.) gives the corresponding oxirane and/or azoxy derivatives, and reaction with OsO4 or other oxidants (e.g., KMnO4) gives the diol or hydroxyketone derivatives (Houben-Weyl, 4/1b, 604 et seq. and 861 et seq.).
If the compounds oxidized with per-acids contain thiolether groups, the sulfone or sulfoxy derivatives are formed.
The oxirane, sulfone or sulfoxy derivatives of V may be prepared from the corresponding derivatives of III in analogy to the conversion of III→V.
5. Manufacture of the compounds described in Example 7 and the table pertaining thereto.
Reaction of compounds III to VII with S4 N4.
Compounds III to VII react with S4 N4 in inert solvents at 80° to 130° C. to give the corresponding cyclic 5-membered trithiolane derivatives.
6. Manufacture of compound VI and the starting compounds described in Example 8 and the table pertaining thereto.
The reaction of compounds IV or VI with carboxylic or thiocarboxylic acid halides, carboxylic acid anhydrides, chlorocarbonic or thiochlorocarbonic acid ester, phosgene, sulfonyl halides, sulfynyl halides, alkyl, alkenyl, alkynyl or aralkyl halides, aldehydes or ketones, isocyanates, mustard oils, and carbamoyl or thiocarbamoyl halides gives the corresponding N-substituted or N,N'-disubstituted derivatives as a result of hydrogen halide elimination or addition of the N--H group on to the C═O or C═N double bond.
These reactions are carried out in accordance with the art, in inert solvents and usually in the presence of bases, e.g., tertiary amines, alkali metal carbonates or bicarbonates, sodium methylate, sodium hydride, alkali metal hydroxides, etc., at from 20° to 130° C.
Reaction of quadricyclane with alkyl-, aryl- or aralkylazodicarboxylic acid diesters gives the corresponding N,N'-disubstituted derivatives.
The compounds listed under 6. can be further reacted as described above under 1. to 5. (Examples 1, 2, 4, 5, 6 and 7).
The structure of the active ingredients was confirmed by nmr, infrared or mass spectroscopy, or by elemental analysis.
The melting and decomposition points given are uncorrected.
At 10° C., 25 parts (by weight) of aqueous NaOCl (about 13% free chlorine) is dripped into 10 parts of V and 8.3 parts of pivalylaldoxime in 100 parts of CH2 Cl2. The organic phase is separated, dried with MgSO4 and concentrated at 25° C. and 15 mm Hg. Yield: 14 parts (77% of theory). Melting point: 132° C. (decomposes) (ligroin). ##STR17##
32 parts of p-methoxychlorobenzaldoxime is added to 20.6 parts of V, 196 parts of triethylamine and 400 parts of ether; the mixture is stirred for 12 hours at 25° C. The solid is filtered, washed with 100 parts of water and dried. Yield: 25.2 parts (55% of theory). Melting point: 160° C. (decomposes) (toluene/ligroin).
The folling compounds were prepared in accordance with Example 1:
__________________________________________________________________________
##STR18##
R A m.p. [°C.]
__________________________________________________________________________
CH.sub.3 NN 98
"
##STR19## 80
*
"
##STR20## 128
"
##STR21## *
(CH.sub.3).sub.3 C
##STR22## 140
"
##STR23## 145
*
##STR24## NN 115
"
##STR25##
" NN
n-C.sub.11 H.sub.23
"
"
##STR26## *
"
##STR27##
C.sub.6 H.sub.5
NN 173
p-BrC.sub.6 H.sub.4
" 196
"
##STR28## 141
*
p-ClC.sub.6 H.sub.4
NN 185
(decomposes)
"
##STR29## 214
*
(decomposes)
"
##STR30## 60
"
##STR31## *
p-CH.sub.3C.sub.6 H.sub.4
NN 181
(decomposes)
p-NO.sub.2C.sub.6 H.sub.4
" 212
(decomposes)
"
##STR32## 167
*
"
##STR33## 169
(CH.sub.3).sub.2 NC.sub.6 H.sub.4
NN 182
(decomposes)
##STR34## "
"
##STR35## 161
##STR36## " 205
(decomposes)
##STR37## " 93
*
" NN 80
"
##STR38## *
##STR39## N N 185
(decomposes)
##STR40## " 110
(decomposes)
"
##STR41## 120
##STR42## *
##STR43##
##STR44## 160
" NN 148
(decomposes)
"
##STR45## 150
"
##STR46## *
##STR47## NN 125
"
##STR48## *
##STR49## NN
"
##STR50##
##STR51## NN 216
(decomposes)
##STR52##
##STR53## *
__________________________________________________________________________
* position isomers
3.6 parts of V and 6 parts of diphenyldiazomethane are stirred for 6 hours in 35 parts of toluene at 80° C. After cooling, the solid is filtered and washed with 50 parts of petroleum ether. Yield: 5.8 parts (61% of theory). Melting point: 203° C. (decomposes) (toluene/ligroin). ##STR55##
5 parts of the p-chlorophenyl-Δ1 -pyrazoline derivative of V is stirred in 100 parts of acetic acid for 4 hours at 60° C. After the solution has cooled, it is treated with 0.5 part of activated carbon and, after filtration, concentrated at 50° C. and 15 mm Hg. The residue is washed with 50 parts of petroleum ether. Yield: 4.2 parts (75% of theory). Melting point: 197° C. (decomposes). ##STR56##
13 parts of V and 23 parts of benzophenyl hydrazide chloride are heated in 100 parts of toluene at 80° C., and 40 parts of triethylamine is slowly added. After 3 hours, the reaction mixture is cooled to 25° C. and filtered. The residue is washed with 100 parts of water and dried. Yield: 17 parts (55% of theory). Melting point: 178° C. (decomposes) (toluene/ligroin). ##STR57##
5 parts of the diphenylpyrazoline derivative is heated in 100 parts of xylene for 15 hours at 140° C. The solvent is then distilled off at 40° C. and 20 mbars, and the residue is washed with 50 parts of petroleum ether. Yield: 4.1 parts (90% of theory). Melting point: 181° C. (toluene/ligroin).
The following compounds were prepared similarly to Examples 2A to C:
__________________________________________________________________________
##STR58##
##STR59##
Formula
R' R A m.p. [°C.]
__________________________________________________________________________
I H H NN 112
(decomposes)
" " "
##STR60## 156
(decomposes)
" CH.sub.3 "
##STR61## *
" " " NN
II H C.sub.2 H.sub.5 OCO
" 134
(decomposes)
" " "
##STR62## 82
*
" " "
##STR63## 135
(decomposes)
" " "
##STR64## 143
(decomposes)
" "
##STR65## NN 137
(decomposes)
" C.sub.2 H.sub.5 OCO
" " 135
(decomposes)
" " "
##STR66## 192
I CH.sub.3 " NN
" CH.sub.2CHCH.sub.2
C.sub.2 H.sub.5 OCO
##STR67## *
" C.sub.6 H.sub.5CH.sub.2
"
##STR68## *
" C.sub.6 H.sub. 5
H NN 172
(decomposes)
" " C.sub.6 H.sub.5
##STR69## 217
*
II " CH.sub.3 NN (decomposes)
" p-ClC.sub.6 H.sub.4
HCO " 148
(decomposes)
" " "
##STR70##
I C.sub.6 H.sub.5
C.sub.6 H.sub.5
" 130
(decomposes)
II " "
##STR71## 185
(decomposes)
" " "
##STR72## 182
(decomposes)
" CH.sub.3 " NN
##STR73##
##STR74##
##STR75## *
I p-ClC.sub.6 H.sub.4
H NN 149
(decomposes)
" " "
##STR76## 90
*
II "
##STR77##
##STR78##
" " " NN
" "
##STR79## "
" " "
##STR80##
" "
##STR81## "
" " " NN
" "
##STR82##
##STR83##
" " " NN
" " C.sub.6 H.sub.5
"
" "
##STR84## "
" " "
##STR85##
I p-CH.sub.3C.sub.6 H.sub.4
H
##STR86## 91
*
(decomposes)
" " "
##STR87## 230
*
" p-ClC.sub.6 H.sub.4
"
##STR88## 156
(decomposes)
" m-NO.sub.2C.sub.6 H.sub.4
" NN
"
##STR89## "
##STR90## *
"
##STR91## " NN
"
##STR92##
##STR93## 98
"
##STR94## H NN
" " "
##STR95## *
II C.sub.2 H.sub.5 OCO
C.sub.6 H.sub.5 SO.sub.2
##STR96##
" p-ClC.sub.6 H.sub.4
##STR97## NN
" C.sub.2 H.sub.5 OCO
##STR98##
##STR99##
" C.sub.6 H.sub.5
C.sub.6 H.sub.5
##STR100## *
" p-ClC.sub.6 H.sub.4
p-ClC.sub.6 H.sub.4
NN
" C.sub.2 H.sub.5 OCO
##STR101## NN
"
##STR102## C.sub.6 H.sub.5
"
" " "
##STR103## *
"
##STR104## " NN
" " "
##STR105##
"
##STR106## p-ClC.sub.6 H.sub.4
NN
" " "
##STR107## *
I
##STR108## H NN
" " "
##STR109##
"
##STR110## " "
" " " NN
II
##STR111## C.sub.6 H.sub.5
"
" " "
##STR112##
" " CH.sub.3 "
" " " NN
" " "
##STR113## *
__________________________________________________________________________
*position isomers
The following compounds were prepared in accordance with Examples 2A and D:
__________________________________________________________________________
##STR114##
R R' A m.p. [°C.]
__________________________________________________________________________
##STR115## NN 186 (decomposes)
##STR116## 270
"
##STR117## 166
"
##STR118## 243
"
##STR119## 92
"
##STR120##
"
##STR121##
"
##STR122##
C.sub.6 H.sub.5
C.sub.6 H.sub.5
NN
C.sub.6 H.sub.5
C.sub.6 H.sub.5
##STR123##
CH.sub.2CHCH.sub.2
##STR124##
##STR125##
C.sub.6 H.sub.5CH.sub.2
##STR126##
NN
CH.sub.3
##STR127##
##STR128##
CH.sub.3 CH.sub.3
##STR129##
" " NN
CH.sub.3 CH.sub.3
##STR130##
C.sub.6 H.sub.5
" "
" " NN
" "
##STR131##
##STR132##
##STR133##
"
##STR134##
__________________________________________________________________________
5 parts of VII and 3.4 parts of p-bromophenyl azide are stirred for 6 hours in 40 parts of toluene at 80° C. After cooling, the Δ1 -1,2,3-triazoline derivative which has formed (position isomers) is filtered and washed with 50 parts of petroleum ether. Yield: 7.4 parts (88% of theory). Melting point: 208° C. (decomposes). ##STR136##
6.8 parts of the above Δ1 -1,2,3-triazoline derivative (isomer mixture) is stirred for 4 hours in 25 parts of acetic acid and 25 parts of ether at 25° C. The aziridine derivative is filtered and washed with 20 parts of ether. Yield: 6.1 parts (90% of theory). Melting point: 228° C.
The following compounds were prepared in accordance with Example 3:
______________________________________
##STR137##
##STR138##
Formula I Formula II
Formula
R m.p. [°C.]
______________________________________
II CH.sub.3SO.sub.2 101*
I C.sub.3 H.sub.7 105 (decomposes)
II C.sub.4 F.sub.9SO.sub.2
172 (decomposes)
I C.sub.12 H.sub.25 126*
(decomposes)
##STR139## *
"
##STR140## *
" C.sub.6 H.sub.5CH.sub.2
185*
"
##STR141## 196* (decomposes)
"
##STR142## *
" p-ClC.sub.6 H.sub.4CH.sub.2
120*
(decomposes)
" C.sub.6 H.sub.5 200*
(decomposes)
II "
" C.sub.6 H.sub.5SO.sub.2
237 (decomposes)
" p-ClC.sub.6 H.sub.4SO.sub.2
214
I p-FC.sub.6 H.sub.4 185*
(decomposes)
"
##STR143## 230* (decomposes)
" " 236*
" m-CF.sub.3C.sub.6 H.sub.4
*
I
##STR144## 174* (decomposes)
"
##STR145## 216* (decomposes)
"
##STR146## *
II
##STR147##
I
##STR148## *
"
##STR149## 199* (decomposes)
II
##STR150## 242
I
##STR151## 195*
"
##STR152## *
II
##STR153##
I
##STR154## 115* (decomposes)
II "
I
##STR155## *
"
##STR156## 141* (decomposes)
"
##STR157## 153* (decomposes)
II
##STR158## 176*
I
##STR159## *
I
##STR160## 149* (decomposes)
II "
I
##STR161## 185* (decomposes)
II
##STR162## 326 (decomposes)
I
##STR163## *
______________________________________
* position isomers
13.5 parts of VII and 19 parts of C,N-phenylnitrone are heated in 150 parts of toluene for 36 hours at 110° C. The mixture is then cooled to 25° C., extracted twice with 50 parts of water, dried with MgSO4 and concentrated at 40° C. and 20 mbars. The residue is washed with 50 parts of a 1:2 mixture of ether and petroleum ether. Yield: 2.3 parts (71% of theory). Melting point: 194° C. (toluene/ligroin). ##STR165##
2.1 parts of III and 3 parts of the azomethinimine derivative are heated in 40 parts of toluene for 72 hours at 100° C. After the toluene has been distilled off at 30° C. and 15 mbars, the residue is washed with 50 parts of a 1:2 mixture of ether and petroleum ether. Yield: 3.6 parts (70% of theory). Melting point: 155° C.
The following compounds were prepared in accordance with Example 4:
__________________________________________________________________________
##STR166##
##STR167##
Formula I Formula II
For- m.p.
mula
R R' R" R"' A [°C.]
__________________________________________________________________________
I C.sub.6 H.sub.5
H C.sub.6 H.sub.5
--
##STR168## 98 *
" " " " -- NN 76 *
" p-ClC.sub.6 H.sub.4
" " --
##STR169## 230 *
" " " " --
##STR170## 89 *
" " " " -- NN 195 *
(de-
II C.sub.6 H.sub.5
C.sub.6 H.sub.5
" NC " com-
po-
ses)
" " " " "
##STR171## *
" " " " "
##STR172##
I CH.sub.3 H p-ClC.sub.6 H.sub.5
-- NN *
" " "
##STR173##
-- " *
" " " " --
##STR174## *
" n-C.sub.3 H.sub.7
" " --
##STR175## *
" " " " -- NN *
" C.sub.6 H.sub.5
" CH.sub.3 -- NN *
##STR176## " C.sub.6 H.sub.5
--
##STR177## *
" " " " -- NN *
I C.sub.6 H.sub.5
H C.sub.6 H.sub.5
--
##STR178## *
"
##STR179## " " -- NN *
"
##STR180## " " --
##STR181## *
" " " " -- NN *
"
##STR182## " " -- NN *
"
##STR183## " " --
##STR184## *
" " " " -- NN *
" " " " --
##STR185## *
"
##STR186## " " -- " *
" " " " -- NN *
"
##STR187## " CH.sub.3 -- NN *
"
##STR188## " C.sub.6 H.sub.5
-- " *
" " " " --
##STR189## *
" " " " --
##STR190## *
"
##STR191## " " --
##STR192## *
" " " " -- NN *
II
##STR193## p-ClC.sub.6 H.sub.4
NC
##STR194## 155
" " " " "
##STR195## 204 *
" " " " " NN
I C.sub.6 H.sub.5
" C.sub.6 H.sub.5
--
##STR196## *
II H R' + R" =
##STR197##
p-NO.sub.2C.sub.6 H.sub.4
##STR198##
" " " " "
##STR199## *
I " R' + R" =
##STR200##
-- " *
" " " " -- NN *
" " "
##STR201##
--
##STR202## *
" " " " --
##STR203## *
" " " " --
##STR204## *
" " R' + R" =
##STR205##
--
##STR206## *
" " " " --
##STR207## *
" " " " -- NN *
"
##STR208## H C.sub.6 H.sub.5
-- NN *
"
##STR209## " " --
##STR210## *
"
##STR211## " " --
##STR212## *
I
##STR213## H C.sub.6 H.sub.5
--
##STR214## 193 *
" " " " --
##STR215## *
" " " " -- NN 103 *
"
##STR216## " " -- " *
" " " CH.sub.3 --
##STR217## *
" " " " -- NN *
"
##STR218## " C.sub.6 H.sub.5
-- " *
" " " " --
##STR219## *
" " " " --
##STR220## *
"
##STR221## " " -- " *
" " " " -- NN *
" " " " --
##STR222## *
" " "
##STR223##
-- NN *
" " " " --
##STR224## *
__________________________________________________________________________
* isomers
5.4 parts of the N-p-chlorophenyl-1 -1,2,3-triazoline derivative is heated in 7 parts of 47% strength aqueous HBr and 50 parts of water for 5 hours at 100° C. After cooling, the solid is filtered and washed with 200 parts of water. Yield: 5.7 parts (88.5% of theory). Melting point: 185° C. (decomposes). ##STR226##
At -10° C., 10.1 parts of bromine in 25 parts of CH2 Cl2 is dripped into 15 parts of III and 50 parts of CH2 Cl2. The solution is stirred for 1 hour at -10° C., then treated with 0.5 part of activated carbon and filtered, and the filtrate is concentrated at 25° C. and 15 mm Hg. The residue is washed with 40 parts of petroleum ether. Yield: 20 parts (80% of theory). Melting point: 103° C. ##STR227##
3.2 parts of V and 2 parts of 2-nitrophenylsulfenyl chloride are heated for 4 hours in 120 parts of CCl4 at 76° C. After cooling, the precipitated solid is filtered and washed with 50 parts of petroleum ether. Yield: 4.0 parts 77% of theory). Melting point: 168° C. (decomposes) (toluene/ligroin). ##STR228##
10 parts of III is dissolved in 100 parts of ether and 50 parts of dichloromethane, and NO and air (40-80 ml/min) are passed in, while stirring, for 1 hour at 0° to 15° C. The precipitate is filtered and washed with 100 parts of ether. Yield: 9.5 parts (72% of theory). Melting point: 120° C. (decomposes). ##STR229##
10 parts of the dimeric nitroso compound is heated in 25 parts of dimethylformamide for 30 minutes at 130° C., and the mixture is then poured into 200 parts of water. The water is extracted twice with 100 parts of dichloromethane. The organic phase is dried with MgSO4 and concentrated at 30° C. and 20 mbars. Yield: 8 parts (80% of theory) of a yellow oil.
The following compounds were prepared in a manner similar to that described in Example 5:
__________________________________________________________________________
##STR230##
##STR231##
Formula I Formula II
Formula
R R' R" R'"
A m.p. [°C.]
__________________________________________________________________________
I Cl H Cl H NN 93
" " " " "
##STR232## 55*
" " " " "
##STR233## 45
" Br " Br "
##STR234## 16
" " " " " NN 83
" " " HO "
##STR235##
" " " " " NN
" " " " "
##STR236##
" H " H Br
##STR237##
" " " " " NN
" " " " Cl "
" " " " I "
" " " " Cl
##STR238##
" " " " I "
II Br " -- -- NN b.p. (0.5 mm)
57
" Cl " -- -- " b.p. (3 mm)
55
I F " H H
##STR239##
" " " " NN
" Br " " "
##STR240## *
" " " " "
##STR241## *
" " " " "
##STR242##
" ON " O.sub.2 N
" NN 95 (decom-
poses)
" " " " "
##STR243##
" Cl " Cl "
##STR244## 35*
" Br " Br "
##STR245## 141*
" ON " O.sub.2 N
" " 116 *
(decom-
poses)
" Br " Br "
##STR246## 5*
" Cl " Cl "
##STR247## 85*
" Br " Br "
##STR248## *
" CFCl.sub.2S
" Cl "
##STR249##
" " " " " NN
" Br " Br "
##STR250## 91
" " " " "
##STR251## 127*
" Cl " CF.sub.3S
" NN
" " " " "
##STR252## *
" " "
##STR253##
"
##STR254## 79
" " " " "
##STR255## 194*
" Br " Br "
##STR256## 21
##STR257##
" Cl " NN 145 (decom- poses)
" " " " "
##STR258## *
" " " " "
##STR259## *
" CF.sub.3S " " " "
" " " " "
##STR260## *
"
##STR261##
" " "
##STR262## *
" " " " "
##STR263## *
" CF.sub.3S " " "
##STR264## *
" I " N.sub.3
"
##STR265## 11
" " " " " NN
" " "
##STR266##
"
##STR267## *
" O.sub.2 N "
##STR268##
" " *
" " " " " NN *
"
##STR269##
" Cl " " 193 (decom- poses)
" " " I " " 183 (decom-
poses)
" " " HO " " 214 (decom-
poses)
"
##STR270##
" Br " "
" " " I " "
"
##STR271##
" CH.sub.3COO
" " 166 (decom- poses)
" " " " "
##STR272##
"
##STR273##
" Cl " NN 158 (decom- poses)
" " " F " "
" " " Br "
##STR274## 110
" " " F " "
" " " Br "
##STR275## 95
" " " " "
##STR276## 90
" " " I "
##STR277## *
"
##STR278##
" Cl "
##STR279## *
" " " HO " " *
" " " " " N N 216 (decom-
poses)
"
##STR280##
" Br " "
"
##STR281##
" I " "
"
##STR282##
" Br " " 161 (decom- poses)
" " " Cl " " 143 (decom-
poses)
"
##STR283##
" Br "
##STR284##
"
##STR285##
" " " "
"
##STR286##
" " " NN 148 (decom- poses)
" " " I " " 146 (decom-
poses)
"
##STR287##
" Br "
##STR288## 239 (decom- poses)
"
##STR289##
" " " "
" " " " " NN
"
##STR290##
" Cl " "
" " " I "
##STR291##
"
##STR292##
" Cl " NN 100 (decom- poses)
"
##STR293##
" Br " " 151 (decom- poses)
" " " " "
##STR294##
" " " Cl " NN 153 (decom-
poses)
" " " I " " 95
"
##STR295##
" Br " "
"
##STR296##
" Cl " "
" " " Br "
##STR297##
"
##STR298##
" Cl " NN 204 (decom- poses)
" " " Br " " 206 (decom-
poses)
"
##STR299##
" Br " "
"
##STR300##
" " " "
" " " " "
##STR301##
__________________________________________________________________________
*position isomers
30 parts of III and 43.5 parts of 3-chloroperbenzoic acid (3-Cl-PBS, 70% strength) are stirred for 6 hours in 800 parts of 1,1,2-trichloroethane at 70° C. After cooling, the solution is filtered and extracted with 250 parts of each of a saturated aqueous KI, Na2 S2 O3 and a NaHCO3 solution. The organic phase is dried with MgSO4 and concentrated at 25° C. and 15 mm Hg. The residue is washed with 100 parts of petroleum ether. Yield: 27.8 parts (87% of theory). Melting point: 130° C. (benzene/ligroin). ##STR303##
1.5 parts of the dibromo derivative of V and 2.7 parts of 3-chlorobenzoic acid (70% strength) are stirred for 2 hours in 20 parts of 1,1,2-trichloroethane at 70° C. After cooling, the solution is filtered and extracted with 30 parts of each of a saturated aqueous KI, Na2 S2 O3 and a NaHCO3 solution. The organic phase is dried with MgSO4 and concentrated at 25° C. and 15 mm Hg. The residue is washed with 10 parts of petroleum ether. Yield: 1.2 parts (78% of theory). Melting point: 116° C. ##STR304##
1.4 parts of V and 3 parts of OsO4 are stirred in 50 parts of ether for 16 hours. The residue is filtered and stirred with 3 parts of mannite and 30 parts of 10% strength KOH for 3 hours. The mixture is then extracted for 48 hours with 200 parts of dichloromethane. The organic phase is concentrated at 30° C. and 20 mbars. Yield: 1.1 parts (52% of theory). Melting point: 153° C. (decomposes).
The following compounds were prepared in a manner similar to that described in Example 6:
__________________________________________________________________________
##STR305##
Formula
R R' A m.p. [°C.]
__________________________________________________________________________
I H H NN 169
(decomposes)
" " "
##STR306## 77
" " "
##STR307##
III Cl
##STR308## NN 145
(decomposes)
" " "
##STR309##
I H H
##STR310## 60
" " "
##STR311## 171
III Cl Cl
##STR312## *
" " CF.sub.3SO.sub.2
NN
##STR313## Cl "
I H H
##STR314## 52
III Cl
##STR315##
##STR316##
" "
##STR317##
##STR318## 199
* (decomposes)
" " "
##STR319## *
" " CFCl.sub.2SO.sub.2
NN
I H H
##STR320## 147
II Br " O 20
*
" Cl " " *
III
##STR321## Cl NN
" " "
##STR322## *
" " "
##STR323##
II H H
##STR324## 235
(decomposes)
" " "
##STR325##
" " "
##STR326##
" " "
##STR327## 244
(decomposes)
" " "
##STR328##
III Cl
##STR329##
##STR330##
" " "
##STR331## *
" Cl
##STR332## NN
II H H
##STR333## 160
* (decomposes)
" " "
##STR334## *
III CFCl.sub.2SO.sub.2
Cl
##STR335## *
" " "
##STR336##
II H H
##STR337## *
" " "
##STR338## 198
(decomposes)
" " "
##STR339## *
" " "
##STR340## *
" " "
##STR341## *
" " "
##STR342## 196
* (decomposes)
" " "
##STR343## *
" " "
##STR344## *
" " "
##STR345## *
" " "
##STR346## 249
* (decomposes)
III Cl CF.sub.3SO.sub.2
##STR347## *
" " "
##STR348##
" " CFCl.sub.2SO "
" " " NN
" " CF.sub.3SO
##STR349##
" " " NN
"
##STR350##
##STR351##
##STR352##
"
##STR353##
##STR354## "
"
##STR355##
##STR356## "
"
##STR357##
##STR358## "
"
##STR359##
##STR360## "
"
##STR361##
##STR362## "
"
##STR363##
##STR364## "
"
##STR365##
##STR366## "
__________________________________________________________________________
*position isomers
23.8 parts of III and 18.4 parts of S4 N4 are heated at 110° C. for 24 hours in 150 parts of toluene. After cooling, the reaction mixture is concentrated almost to dryness at 0° C. and 5 mm Hg and the residue is recrystallized from ligroin. Yield: 18.4 parts (55% of theory). Melting point: 210° C. (decomposes).
The following compounds were prepared in the same way: ##STR368##
Manufacture of starting materials (not in accordance with the invention) ##STR369##
While stirring and at 65° C., a solution of 35 parts of KOH in 60 parts of methanol is dripped into 60 parts of compound III and 50 parts of methanol. The reaction mixture is then stirred for 2 hours at 65° C. The solvent is then distilled off at 50 mbars and the residue extracted several times with a total of 1,200 parts of ether. After the ether has been distilled off, there is obtained 38 parts (85% of theory) of compound VI; m.p.: 94° C. (from ligroin). ##STR370##
5 parts of compound VI, 7 parts of p-chlorobromoacetophenone and 3 parts of soda are stirred in 150 parts of ether for 24 hours at 34° C. After filtration of the inorganic salts, the solvent and the residue are washed with 50 parts of petroleum ether. Yield: 9.5 parts (91% of theory). Melting point: 111° C. (benzene/ligroin). ##STR371##
17 parts of compound VI and 8.7 parts of methyl-mustard oil are heated in 200 parts of benzene for 5 hours at 80° C. After the solvent has been distilled off, the residue is washed with 100 parts of petroleum ether. Yield: 25 parts (97% of theory). Melting point: 116° C. (ethanol/ligroin). ##STR372##
At 80° C., 40.5 parts of azodicarboxylic acid dissopropyl ester is dripped into 20 parts of quadricyclane in 100 parts of benzene. The mixture is then heated for 24 hours at 80° C. and the solvent is then removed at 50 mbars. Yield: 58 parts (98% of theory). Melting point: 41° C.
The following compounds were prepared in the same way:
__________________________________________________________________________
##STR373##
R.sub.1 R.sub.2 m.p. [°C.]
__________________________________________________________________________
##STR374## 163 (decomposes)
CH.sub.2COOCH.sub.3 COOCH.sub.3 76
SO.sub.2C.sub.6 H.sub.5
" 130
##STR375## " 128
##STR376## " 141
##STR377## " 164 (decomposes)
##STR378## " 128
##STR379## " b.p. (1 mbar) 100
##STR380## " 73
##STR381## " 75
##STR382## " -10
##STR383## " 135
##STR384##
##STR385## 98
##STR386##
##STR387## 12
__________________________________________________________________________
The compounds described in Example 8 and the table pertaining thereto may be used as starting compounds for the synthesis of active ingredients (cf. tables in Examples 1, 2, 4, 5, 6 and 7).
The new active ingredients have a strong biological action on plants, i.e., they influence plant growth, either by reducing growth height, by changing the concentration of plant materials, or by destroying unwanted plants while leaving crop plants unaffected.
Application may be effected for instance in the form of directly sprayable solutions, powders, suspensions, dispersions, emulsions, oil dispersions, pastes, dusts, broadcasting agents, or granules by spraying, atomizing, dusting, broadcasting or watering. The forms of application depend entirely on the purpose for which the agents are being used; in any case they should ensure a fine distribution of the active ingredient.
For the preparation of solutions, emulsions, pastes and oil dispersions to be sprayed direct, mineral oil fractions of medium to high boiling point, such as kerosene or diesel oil, further coal-tar oils, etc. and oils of vegetable or animal origin, aliphatic, cyclic and aromatic hydrocarbons such as benzene, toluene, xylene, paraffin, tetrahydronaphthalene, alkylated naphthalenes and their derivatives such as methanol, ethanol, propanol, butanol, chloroform, carbon tetrachloride, cyclohexanol, cyclohexanone, chlorobenzene, isophorone, etc., and strongly polar solvents such as dimethylformamide, dimethyl sulfoxide, N-methylpyrrolidone, water, etc. are suitable.
Aqueous formulations may be prepared from emulsion concentrates, pastes, oil dispersions or wettable powders by adding water. To prepare emulsions, pastes and oil dispersions the ingredients as such or dissolved in an oil or solvent may be homogenized in water by means of wetting or dispersing agents, adherents or emulsifiers. Concentrates which are suitable for dilution with water may be prepared from active ingredient, wetting agent, adherent, emulsifying or dispersing agent and possibly solvent or oil.
Examples of surfactants are: alkali metal, alkaline earth metal and ammonium salts of ligninsulfonic acid, naphthalenesulfonic acids, phenolsulfonic acids, alkylaryl sulfonates, alkyl sulfates, and alkyl sulfonates, alkali metal and alkaline earth metal salts of dibutylnaphthalenesulfonic acid, lauryl ether sulfate, fatty alcohol sulfates, alkali metal and alkaline earth metal salts of fatty acids, salts of sulfated hexadecanols, heptadecanols, and octadecanols, salts of sulfated fatty alcohol glycol ethers, condensation products of sulfonated naphthalene and naphthalene derivatives with formaldehyde, condensation products of naphthalene or naphthalenesulfonic acids with phenol and formaldehyde, polyoxyethylene octylphenol ethers, ethoxylated isooctylphenol, ethoxylated octylphenol and ethoxylated nonylphenol, alkylphenol polyglycol ethers, tributylphenol polyglycol, ethers, alkylaryl polyester alcohols, isotridecyl alcohols, fatty alcohol ethylene oxide condensates, ethoxylated castor oil, polyoxyethylene alkyl ethers, ethoxylated polyoxypropylene, lauryl alochol polyglycol ether acetal, sorbitol esters, lignin, sulfite waste liquors and methyl cellulose.
Powders, dusts and broadcasting agents may be prepared by mixing or grinding the active ingredients with a solid carrier.
Granules, e.g., coated, impregnated or homogeneous granules, may be prepared by bonding the active ingredients to solid carriers. Examples of solid carriers are mineral earths such as silicic acid, silica gels, silicates, talc, kaolin, Attaclay, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth, calcium sulfate, magnesium sulfate, magnesium oxide, ground plastics, fertilizers such as ammonium sulfate, ammonium phosphate, ammonium nitrate, and ureas, and vegetable products such as grain flours, bark meal, wood meal, and nutshell meal, cellulosic powders, etc.
The formulations contain from 0.1 to 95, and preferably 0.5 to 90, % by weight of active ingredient.
There may be added to the compositions or individual active ingredients oils of various types, herbicides, fungicides, nematocides, insecticides, bactericides, trace elements, fertilizers, antifoams (e.g., silicones), and other growth regulators.
In various cases, it may prove advantageous to combine or mix the compounds according to the invention with other growth-regulating active ingredients, e.g., ethylene-forming compounds of various chemical structures (such as phosphonic acid derivatives, silanes, ethyl hydrazines), and onium compounds (such as trimethylammonium, hydrazonium and sulfonium salts, and derivatives of morpholinium, piperidinium and pyridazinium compounds). Other growth-regulating substances, e.g., from the group of trifluoromethylsulfonamido-p-acetotoluidides, maleic hydrazide, abscisin derivatives, chlorinated phenoxy fatty acids having an auxin-like action, and polyhydric alcohols and fatty acid esters having a specific action on meristematic tissue.
The application rate of the agents according to the invention may vary, and depends mainly on the type of effect desired; it is generally from 0.1 to 15 more more, but preferably from 0.2 to 6, kg of active ingredient per hectare.
The agents according to the invention influence the growth of plant parts above and below the soil in different ways, and have, at the usual application concentrations, a low toxicity to warmbloods.
The new agents have an effect on the physiology of plants, and may be used for various purposes. The different actions of these active ingredients depend in essence on the time of application, with reference to the development stage of the seed or plant, and on the concentrations employed.
Vegetative and generative plant growth, and--in appropriate concentrations--germination are influenced by the new agents.
The influence on vegetative development is manifested particularly in a reduction in growth height, resulting in many plants, particularly cereals, in increased rigor and a reduced tendency to lodging. Tillering is also improved, which results in a larger number of ear-bearing stems per unit area.
In grass, the reduction in growth height results in a more compact and resistant sward, and especially in a reduction in mowing frequency. This is of great economic advantage with lawns, grass verges and in parks. An additional feature is that, parallel to the reduction in growth height, the chlorophyll content of the plant is also increased; consequently, grass and other plants treated with the new agents take on a much darker green.
The influence on vegetative growth results in numerous plants, e.g., cotton and soybeans, in a considerable increase in flowering and fruiting.
Attention should be drawn in particular to the surprising fact that treatment with the compounds according to the invention induces rooting. This results in more rational utilization of water and nutrients by the treated plants; their resistance to dryness and cold (frost) is also increased.
The agents according to the invention may also find varied and extensive use in fruit crops, the cultivation of ornamentals and landscape gardening, including the influence of vegetation on uncultivated areas, airfields and training areas.
The compounds may also be successfully used to influence blossoming and ripening, and in special cultivation processes.
The new agents may also influence the concentration of important plant materials such as sugar and proteins.
The extent and type of action are dependent on various factors, especially the time of application with reference to the development stage of the plant, and the concentration. These factors in turn vary, depending on the type of plant and the desired effect. Thus, for instance, lawns should be treated during the whole growth period; ornamentals in which it is desired to increase the intensity and number of flowers, before the buds have formed; and plants whose fruit is to be eaten or processed, a sufficient length of time before the harvest. Various derivatives of the class of compounds described here have herbicidal properties. They are therefore suitable for removing unwanted plant growth, or keeping it in check.
Influence of some polycyclic nitrogenous compounds on the growth height of wheat and barley
Spring wheat of the "Opal" variety and spring barley of the "Union" variety were grown in the winter half of the year under greenhouse conditions in plastic dishes 11.5 cm in diameter, in a peat substrate provided with sufficient nutrients.
For the soil (preemergence) treatment, the active ingredients were poured, at two application rates, as aqueous formulations onto the final soil surface after sowing.
The reductions in growth height caused by the treatment were determined by measuring the height of the plants at the end of the experiment after 30 days' growth, and comparing it with that of untreated plants. The prior art active ingredient N,N,N-trimethyl-N-β-chloromethylammonium chloride (CCC, German Printed Application DAS No. 1,294,734) was also used for comparison purposes.
The individual results are given in the table below.
______________________________________
Influence on the growth height of spring wheat
Soil treatment
Appln. rate
Plant height
Active Ingredient kg/ha cm %
______________________________________
Control -- 30.0 100
(untreated)
CCC 3 21.5 71.7
(prior art) 12 19.5 65.0
##STR388## 3 12 21.5 12.5
71.7 41.7
##STR389## 3 12 20.0 14.0
66.7 46.7
______________________________________
______________________________________
Influence on the growth height of spring barley
Soil treatment
Appln. rate
Plant height
Active Ingredient kg/ha cm %
______________________________________
Control -- 32.2 100
(untreated)
CCC 3 27.5 85.1
(prior art) 12 24.5 75.9
##STR390## 3 12 25.0 14.0
77.4 43.3
##STR391## 3 12 24.5 16.0
75.9 49.5
______________________________________
Influence of some polycyclic nitrogenous compounds on the growth height of wheat and barley
Spring wheat ("Opal" variety) and spring barley ("Union" variety) were grown under greenhouse conditions in plastic dishes 11.5 cm in diameter, in a peat substrate provided with sufficient nutrients. For the soil (preemergence) treatment, the active ingredients were poured, at two application rates, as aqueous formulations onto the surface of the substrate after sowing.
Leaf treatment was effected by spraying the plants at a growth height of 10 cm with aqueous formulations of the active ingredients at two application rates.
The plant height was measured at the end of the experiment. The figures obtained show the shortening effect of the active ingredients under investigation. The prior art compound β-chloroethylphosphonic acid (Ethephon, German Printed Application DAS No. 1,667,968) was used for comparison purposes.
The individual results are given below:
______________________________________
Influence on the growth height of spring wheat
A Soil treatment
Appln. rate
Plant height
Compound kg/ha cm %
______________________________________
Control -- 32.0 100
(untreated)
Ethephon 3 29.0 90.6
(prior art) 12 25.0 78.1
##STR392## 3 12 17.0 14.0
53.1 43.8
##STR393## 3 12 26.5 25.5
82.8 79.7
##STR394## 3 12 25.5 22.0
79.7 68.8
##STR395## 3 12 23.5 22.0
73.4 68.8
##STR396## 3 12 27.0 24.5
84.4 76.6
##STR397## 3 12 16.0 15.0
50.0 46.9
______________________________________
______________________________________
Influence on the growth height of spring wheat
B Leaf treatment
Appln. rate
Plant height
Compound kg/ha cm %
______________________________________
Control -- 32.8 100
(untreated)
Ethephon 1.5 30.0 91.5
(prior art) 6.0 25.0 76.2
##STR398## 1.5 6.0 23.5 22.0
71.6 67.1
##STR399## 1.5 6.0 29.0 27.5
88.4 83.8
##STR400## 1.5 6.0 29.0 27.0
88.4 82.3
##STR401## 1.5 6.0 29.5 27.5
89.9 83.3
##STR402## 1.5 6.0 29.0 27.0
88.4 82.3
##STR403## 1.5 6.0 27.5 25.5
83.3 77.7
______________________________________
______________________________________
Influence on growth height of spring barley
A Soil treatment
Appln. rate
Plant height
Compound kg/ha cm %
______________________________________
Control -- 34.3 100
(untreated)
Ethephon 3 32.0 93.3
(prior art) 12 27.5 80.2
##STR404## 3 12 22.0 20.0
64.1 58.3
##STR405## 3 12 28.0 26.0
81.6 75.8
##STR406## 3 12 27.0 24.0
78.8 70.0
##STR407## 3 12 25.0 21.0
72.9 61.2
##STR408## 3 12 30.0 29.0
87.5 84.5
##STR409## 3 12 26.0 24.0
75.8 70.0
______________________________________
______________________________________
Influence on growth height of spring barley
B Leaf treatment
Appln. rate Plant height
Compound kg/ha cm %
______________________________________
Control -- 28.0 100
(untreated)
Ethephon 1.5 27.0 96.4
(prior art) 6.0 24.5 87.5
##STR410## 1.5 6.0 22.0 19.5
78.6 69.6
##STR411## 1.5 6.0 25.5 25.0
91.1 89.3
##STR412## 1.5 6.0 25.0 24.5
89.3 87.5
##STR413## 1.5 6.0 25.5 25.0
91.1 89.3
##STR414## 1.5 6.0 26.0 24.5
92.9 87.5
##STR415## 1.5 6.0 25.0 24.0
89.3 85.7
______________________________________
Influence of some polycyclic nitrogenous compounds on the growth height of wheat, barley and rye
The test plants--spring wheat ("Opal" variety), spring barley ("Union" variety) and spring rye ("Petkuser" variety)--were grown under greenhouse conditions in plastic dishes 11.5 cm in diameter, in a peat substrate provided with sufficient nutrients.
The soil (preemergence) treatment was effected after sowing by pouring aqueous formulations of the active ingredients, at four application rates, onto the surface of the substrate.
Leaf treatment was effected by spraying the plants at a growth height of 11 cm with aqueous formulations of the active ingredients, at three application rates.
The shortening effect caused by the compounds was shown by measurements of the height of the plants at the end of the experiment.
The prior art compound N,N,N-trimethyl-N-β-chloroethylammonium chloride (CCC, German Printed Application DAS No. 1,294,734) was used for comparison purposes.
The individual results are given below:
______________________________________
Influence on the growth height of spring wheat
Leaft treatment
Appln. rate
Plant height
Compound kg/ha cm %
______________________________________
Control -- 30.8 100
(untreated)
CCC 0.75 27.5 89.3
(prior art) 1.50 26.0 84.4
3.00 25.0 81.2
##STR416## 0.75 1.50 3.00
26.5 25.5 24.0
86.0 82.8 77.9
______________________________________
______________________________________
Influence on the growth height of spring barley
A Soil treatment
Appln. rate
Plant height
Compound kg/ha cm %
______________________________________
Control -- 32.8 100
(untreated)
CCC 0.75 29.5 89.9
(prior art) 1.50 29.5 89.9
3.00 27.5 83.8
##STR417## 6.00 0.75 1.50 3.00 6.00
26.0 32.0 28.0 27.0 23.0
79.3 97.6 85.4 82.3 70.1
______________________________________
______________________________________
B Leaf treatment
Appln. rate
Plant height
Compound kg/ha cm %
______________________________________
Control -- 27.8 100
(untreated)
CCC 0.75 27.5 98.4
(prior art) 1.50 27.0 97.1
3.00 27.0 97.1
##STR418## 0.75 1.50 3.00
23.5 23.0 21.5
84.5 82.7 77.3
##STR419## 0.75 1.50 3.00
26.0 25.5 23.5
93.5 91.7 84.5
______________________________________
______________________________________
Influence on the growth height of spring rye
A Soil treatment Appln. rate
Plant height
Compound kg/ha cm %
______________________________________
Control -- 32.3 100
(untreated)
CCC 0.75 31.5 97.5
(prior art) 1.50 30.5 94.4
3.00 30.0 92.9
6.00 28.5 88.2
##STR420## 0.75 1.50 3.00 6.00
30.0 26.5 25.0 23.0
92.9 82.0 77.4 71.2
##STR421## 0.75 1.50 3.00 6.00
28.0 27.0 25.0 23.0
86.7 83.5 77.4 71.2
______________________________________
______________________________________
B Leaf treatment Appln. rate
Plant height
Compound kg/ha cm %
______________________________________
Control -- 28.5 100
(untreated)
CCC 0.75 27.0 94.7
(prior art) 1.50 25.5 89.5
3.00 25.5 89.5
##STR422## 0.75 1.50 3.00
23.0 20.5 20.5
80.7 71.9 71.9
##STR423## 0.75 1.50 3.00
25.5 24.5 24.5
89.5 86.0 86.0
______________________________________
Action on grass or lawns
In an experiment in large vessels, lawn seed of the following standard composition was sown in a loamy soil: Agrostis tenuis (10%), Cynosurus cristatus (10%), Festuca rubra (15%), Lolium perenne (35%) and Poa pratensis (30%). 1.5 g of N as ammonium nitrate and 1 g of P2 O5 as secondary potassium phosphate were applied as fertilizer. After the grass had been cut twice, the active ingredients were sprayed in conventional manner at various application rates onto the grass which was 4 cm high. The growth height and the mowings were determined 19 days after the treatment. Compared with the control, the treated plants reacted with most considerable height reductions and a proportionate decrease in mowings.
The data below also demonstrate the lasting action of the agents investigated.
__________________________________________________________________________
Influence on the growth height of, and amount of mowings in, gass
Appln.
First mowing Second mowing
rate
Growth height
Mowings Growth height
Mowings
Compound kg/ha
cm relative
g relative
cm relative
g relative
__________________________________________________________________________
Control -- 21.8
100 134.2
100 20.0
100 90.6
100
##STR424## 3.0 6.0
20.0 17.0
91.7 78.0
116.3 101.1
86.7 75.3
19.0 16.5
95.0 82.5
94.8 85.2
104.6 94.0
##STR425## 3.0 6.0
20.0 18.0
91.7 82.6
125.1 119.0
93.2 88.7
19.0 19.0
95.0 95.0
89.9 92.2
99.2 101.8
##STR426## 3.0 6.0
21.0 18.5
96.3 84.9
117.7 114.0
87.7 84.9
18.5 17.0
92.5 85.0
75.3 72.1
83.1 79.6
__________________________________________________________________________
Experiments demonstrating the growth-regulating or herbicidal action
To demonstrate the effectiveness of the new compounds, greenhouse experiments were carried out as follows. Plastic flowerpots having a volume of 300 cm3 were filled with a sandy loam and the test plants placed therein (either as seed, as vegetatively reproduced species, or as potted plants, e.g., vines). For preemergence treatment, the active ingredients were suspended or emulsified in water as vehicle and sprayed onto the surface of the soil immediately after sowing by means of finely distributing nozzles. The potted vines were treated by spraying them with the correspondingly diluted liquor. For postemergence treatment, the agents were, as stated above, sprayed in water onto the leaves of the test plants, some liquor also falling onto the soil. In some special cases, solid active ingredients were first dissolved in dimethylformamide and then applied in a total liquor amount of 400 liters of water per hectare. For the postemergence treatment, the plants were first grown to a height of from 3 to 10 cm before being treated. With grasses, the first growth was cut, and the new growth treated 2 to 3 days after cutting. The temperature requirements of the plants were taken into account by placing them in cooler or warmer sections of the greenhouse. The experiments were run for from 4 to 6 weeks, during which time the plants were tended and their reaction to the various treatments was assessed.
The application rates are given in kg/ha of active ingredient, regardless of the method of application and the amount of water used.
A 0 to 100 scale was used for the evaluation, 0 denoting normal emergence or no damage (or no inhibition), and 100 denoting non-emergence or complete destruction of the plants. A distinction should be made in the influence on growth between desired changes without any appreciable disadvantageous phytotoxic effects (e.g., purely growth-regulating effects) and those of a phytotoxic herbicical character.
The results are given in the tables below.
______________________________________
List of plant species
Botanical term Common name
______________________________________
Alopecurus myosuroides
Blackgrass
Cynodon dactylon Bermudagrass
Cyperus esculentus Yellow nutsedge
Datura stramonium Jimson weed
Digitaria sanguinalis
Hairy crabgrass
Echinochloa crus galli
Barnyardgrass
Euphorbia spp. Spurge family
usually E. geniculata
Eleusine indica Goosegrass
Galium aparine Catchweed bedstraw
Ipomoea spp. Morningglory
usually I. lacunosa
Matricaria chamomilla
Wild chamomile
Panicum virgatum Switchgrass
Poa annua Annual bluegrass
Setaria faberii Giant foxtail
Sinapis alba White mustard
Solanum nigrum Black nightshade
Sorghum halepense Johnsongrass
Stellaria media Chickweed
______________________________________
______________________________________
Tolerance of new compounds by potted vines in greenhouse;
spray application
Change Potted
in shoot vines -
growth leaf
Compound kg/ha cm damage
______________________________________
##STR427## 4.0 8.0 14.7 13.3
none
##STR428## 4.0 8.0 17.3 10.3
chlorotic yellow- ing, necroses
prior art
##STR429## 4.0 8.0 15.3 15.7
slight chlorosis
prior art
Untreated control -- 15.3 none
______________________________________
__________________________________________________________________________
Removal and inhibition of unwanted plants; pre-(PRE)-emergence treatment
in the greenhouse
Test plants and % damage
Cyper.
Echin.
Lam.
Setar.
Solan.
Compound kg/ha
esc.
c.g.
spp.
spp.
nig.
__________________________________________________________________________
##STR430## 2.0 PRE 4.0 PRE 8.0 PRE
20 55 70
50 80 90
95 95 95
100 100 100
95 95 95
##STR431## 2.0 PRE 4.0 PRE 8.0 PRE
0 0 0
88 90 95
72 90 95
40 100 100
85 85 90
__________________________________________________________________________
0 = no damage
100 = complete destruction
______________________________________
Growth inhibition in lawns caused by new compounds;
preemergence treatment in the greenhouse
% growth inhibition
kg/ after emergence Poa
Compound ha pratensis
______________________________________
##STR432## 0.5 1.0 2.0 4.0
50 60 60 70
very short growth overall; grass compact
nd dark green
prior art 0.5 0
[ClCH.sub.2CH.sub.2N(C.sup.⊕H.sub.3).sub.3 ].sup.⊖ Cl
1.0 10
2.0 10
4.0 10
______________________________________
0 = no inhibition
100 = no growth
______________________________________
Influence on shoot growth of various plants; postemergence
treatment in the greenhouse
Shoot
length
(cm) in
Ara- Ory-
chys za Poa
kg/ hypo- sa- pra-
Compound ha gaea tiva tensis
______________________________________
##STR433## 1.0 2.0 4.0
10 10 10
16 16 16
2.sup.x 2.sup.x 2.sup.x
Control (untreated) 14 22 4
##STR434## 1.0 2.0 4.0
12 5 5 -- -- --
4 4 4
prior art 1.0 16 20 4
[ClCH.sub.2CH.sub.2N.sup.⊕(CH.sub.3).sub.3 ].sup.⊖
2.0 16 20 4
4.0 16 20 3
______________________________________
.sup.x limited leaf scorch
______________________________________
Influence on the shoot growth of various plants; postemergence
treatment in the greenhouse
Shoot length
(cm) in
Eu-
Cy- phor-
no- bia Hor-
don.sup.x
gen-
deum Poa
kg/ dac- icu- vul- pra-
Structural formula
ha tylon lata gare tensis
______________________________________
##STR435## 0.5 1.0 2.0
-- 5 5 9 9 9
12.5 12 12
-- -- --
##STR436## 0.5 1.0 2.0
-- 6 6 -- -- --
16 15 14
-- 13 13
[ClCH.sub.2CH.sub.2N(C.sup.⊕H.sub.3).sub.3 ].sup.⊖ Cl
0.5 -- 12.5 14 --
prior art 1.0 7 13 14 20
2.0 7 13 14 19
Untreated control -- 8 14 19 20
______________________________________
.sup.x from seed
______________________________________
Inhibition of shoot growth by growth regulators;
pre-(PRE) and post(POST)-emergence treatment
in the greenhouse
Test plants and
shoot growth
inhibition (%)
Euphor- Medi-
bia cago
geni- sa-
Structural formula
kg/ha culata tiva
______________________________________
##STR437## 0.5 PRE 1.0 PRE 2.0 POST 4.0 POST
33 40 30 30
-- -- 20 20
[ClCH.sub.2CH.sub.2N(C.sup.⊕H.sub.3).sub.3 ].sup.⊖ Cl
0.5 PRE 0 0
prior art 1.0 PRE 0 0
2.0 POST 0 0
4.0 POST 10 0
______________________________________
__________________________________________________________________________
Influence of growth-regulating compounds on plant growth;
pre-(PRE) and post(POST)-emergence treatment in the greenhouse
Test plants and % shoot inhibition
Arachys
Glycine
Euphorbia
Cynodon.sup.x
Tritic.
Hordeum
Poa
Structural formula kg/ha hypog.
max genic.
dactyl.
aestiv.
vulg.
prat.
__________________________________________________________________________
##STR438## 1.0 PRE 2.0 PRE 1.0 POST 2.0 POST
10 10 20 30
10 25 -- --
10 30 -- --
10 10 13 25
30 30 10 20
25 25 30 30
60 60 60 60
[ClCH.sub.2CH.sub.2N(C.sup.⊕H.sub.3 ).sub.3 ].sup.⊖ Cl
1.0 PRE
0 0 0 0 20 20 0
prior art 2.0 PRE
0 0 0 0 20 20 0
1.0 POST
0 0 0 0 30 10 0
2.0 POST
0 0 0 0 30 10 0
##STR439## 1.0 PRE 2.0 PRE 1.0 POST 2.0 POST
50 50 30 30
0 0 -- --
0 0 -- --
-- -- 20 20
-- -- -- --
-- -- -- --
-- -- -- --
prior art
__________________________________________________________________________
.sup.x from seed
__________________________________________________________________________
Herbicidal action of new compounds; pre-(PRE) and post (POST)-emergence
application in the greenhouse
__________________________________________________________________________
Test plants and % damage
Cynodon
Lolium
Sinapis
Menta
Ipom.
Viola
dact.
Euph.
Compound kg/ha mult.
alba
piper.
spp.
tric.
(seed)
gen.
__________________________________________________________________________
##STR440## 3.0 PRE 3.0 POST
90 95
80 --
-- 100
-- 100
-- 95
-- --
-- --
##STR441## 3.0 POST
-- 100 -- -- -- -- --
##STR442## 3.0 PRE 3.0 POST 1.0 PRE
40 100 --
70 100 --
-- -- --
-- -- --
-- -- --
-- -- 100
-- -- 90
##STR443## 3.0 PRE 3.0 POST 1.0 PRE 2.0 POST
100 100 -- -- -- --
-- -- -- --
-- -- -- --
-- -- 90 100
-- -- 70 95
__________________________________________________________________________
Test plants and % damage
Cynodon
Lolium
Galium
Ipom.
Mentha
dact.
Sinapis
Compound kg/ha mult.
apar.
spp. piper.
(seed)
alba
__________________________________________________________________________
##STR444## 3.0 POST
95 70 95 40 -- --
##STR445## 3.0 PRE 3.0 POST
95 100
-- 60
-- 100
-- 100
-- --
90 --
##STR446## 3.0 POST
-- 30 100 40 -- --
##STR447## 3.0 PRE 3.0 POST
80 85
-- 40
-- 60
-- 95
-- --
80 --
##STR448## 3.0 PRE 3.0 POST
80 100
-- 75
-- 100
-- 100
-- --
100 --
__________________________________________________________________________
Test plants and % damage
Cynodon
dact.
(seed)
appln.
Lolium
Galium
Ipom Mentha
rate Sinapis
Compound kg/ha mult.
apar.
spp. piper.
2 kg/ha
alba
__________________________________________________________________________
##STR449## 3.0 PRE 3.0 POST
95 100
-- 80
-- 100
-- 100
-- 100
100 --
##STR450## 3.0 PRE 3.0 POST
80 100
-- 65
-- 85
-- 95
-- --
100 --
##STR451## 3.0 POST
100 80 80 100 -- --
##STR452## 3.0 PRE 3.0 POST
100 100
-- 90
-- 100
-- 95
-- --
95 --
##STR453## 3.0 PRE 3.0 POST
100 100
-- 95
-- 100
-- 75
-- 100
90 --
__________________________________________________________________________
.sup.x dissolved in dimethylformamide before application
20 parts by weight of compound 1 is well mixed with 3 parts by weight of the sodium salt of diisobutylnaphthalene-α-sulfonic acid, 17 parts by weight of the sodium salt of a lignin-sulfonic acid obtained from a sulfite waste liquor, and 60 parts by weight of powdered silica gel, and triturated in a hammer mill. By uniformly distributing the mixture in 20,000 parts by weight of water, a spray liquid is obtained containing 0.1% by weight of the active ingredient.
3 parts by weight of compound 2 is intimately mixed with 97 parts by weight of particulate kaolin. A dust is obtained containing 3% by weight of the active ingredient.
30 parts by weight of compound 2 is intimately mixed with a mixture consisting of 92 parts by weight of powdered silica gel and 8 parts by weight of paraffin oil which has been sprayed onto the surface of this silica gel. A formulation of the active ingredient is obtained having good adherence.
40 parts by weight of compound 1 is intimately mixed with 10 parts of the sodium salt of a phenolsulfonic acid-urea-formaldehyde condensate, 2 parts of silica gel and 48 parts of water to give a stable aqueous dispersion. Dilution in 100,000 parts by weight of water gives an aqueous dispersion containing 0.04 wt% of active ingredient.
20 parts of compound 1 is intimately mixed with 2 parts of the calcium salt of dodecylbenzenesulfonic acid, 8 parts of a fatty alcohol polyglycol ether, 2 parts of the sodium salt of a phenolsulfonic acid-urea-formaldehyde condensate and 68 parts of a paraffinic mineral oil. A stable oily dispersion is obtained.
90 parts by weight of compound 1 is mixed with 10 parts by weight of N-methyl-α-pyrrolidone. A mixture is obtained which is suitable for application in the form of very fine drops.
20 parts by weight of compound 2 is dissolved in a mixture consisting of 80 parts by weight of xylene, 10 parts by weight of the adduct of 8 to 10 moles of ethylene oxide to 1 mole of oleic acid-N-monoethanolamide, 5 parts by weight of the calcium salt of dodecylbenzenesulfonic acid, and 5 parts by weight of the adduct of 40 moles of ethylene oxide to 1 mole of castor oil. By pouring the solution into 100,000 parts by weight of water and uniformly distributing it therein, an aqueous dispersion is obtained containing 0.02% by weight of the active ingredient.
20 parts by weight of compound 1 is dissolved in a mixture consisting of 40 parts by weight of cyclohexanone, 30 parts by weight of isobutanol, 20 parts by weight of the adduct of 7 moles of ethylene oxide to 1 mole of isooctylphenol, and 10 parts by weight of the adduct of 40 moles of ethylene oxide to 1 mole of castor oil. By pouring the solution into 100,000 parts by weight of water and finely distributing it therein, an aqueous dispersion is obtained containing 0.02% by weight of the active ingredient.
20 parts by weight of compound 1 is dissolved in a mixture consisting of 25 parts by weight of cyclohexanol, 65 parts by weight of a mineral oil fraction having a boiling point between 210° and 280° C., and 10 parts by weight of the adduct of 40 moles of ethylene oxide to 1 mole of castor oil. By pouring the solution into 100,000 parts by weight of water and uniformly distributing it therein, an aqueous dispersion is obtained containing 0.02% by weight of the active ingredient.
Claims (2)
1. A compound of the formula ##STR454## where R3 and R4 are either individual radicals or together form the radical (B)n,
A denotes the radical ##STR455## B denotes the radical ##STR456## when A is ##STR457## B also denotes the radical ##STR458## n is one of the integers 0 and 1, R1 to R27 are identical or different and each denotes hydrogen, with the exception of R3 and R4, or alkyl, with the exception of R6 and R7 and with the proviso that R3 and R4 do not simultaneously denote alkyl, alkenyl or alkynyl of 1 to 30 carbon atoms, phenyl, naphthyl, or the aromatic radical ##STR459## a heterocyclic radical selected from the group consisting of ##STR460## aralkyl or alkyl substituted by one of said heterocyclic radicals; the abovementioned radicals R1 to R27, apart from hydrogen, being unsubstituted or mono- or polysubstituted by halogen, azide, cyanide, cyanate, thiocyanate, --OH, --SH, --NO2, ##STR461## further, R1 and R7 are also selected from the group consisting of halogen, --N3, --CN, --OCN, --SCN, --OH, --SH, --NO2, --NH2, --NO, ##STR462## --N(H,Alk)--N(H,Alk,Ar)2, --COOH or --SO3 H or salts thereof, --SO2 Cl, Alk(Ar)--O--, ##STR463## --SO2 --0Alk(Ar)--, haloalkyl, haloalkoxy, haloalkylmercapto or the radicals ##STR464## and R1 and R3 together, or R2 and R4 together, also denote ═O, ═S, ═NH, ═NAlk(Ar), ═N--OH, ═N--OAlk(Ar), ═C(H,Alk,Ar)2, ##STR465## ═N--N(H,Alk,Ar), wherein Alk is alkyl of 1-30 carbon atoms and Ar is phenyl, naphthyl, ##STR466##
2. A compound selected from the group consisting of compounds of the formulae ##STR467##
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19772742034 DE2742034A1 (en) | 1977-09-19 | 1977-09-19 | POLYCYCLIC NITROGEN COMPOUNDS |
| DE2742034 | 1977-09-19 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US4259235A true US4259235A (en) | 1981-03-31 |
Family
ID=6019282
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US05/941,010 Expired - Lifetime US4259235A (en) | 1977-09-19 | 1978-09-11 | Tricyclic nitrogenous compounds having string plant growth regulating properties |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US4259235A (en) |
| EP (1) | EP0001271B1 (en) |
| JP (2) | JPS54117458A (en) |
| AT (1) | AT359097B (en) |
| AU (1) | AU519224B2 (en) |
| BR (1) | BR7806112A (en) |
| CA (1) | CA1099259A (en) |
| CS (1) | CS200241B2 (en) |
| DD (1) | DD139201A5 (en) |
| DE (2) | DE2742034A1 (en) |
| DK (1) | DK411978A (en) |
| FI (1) | FI782848A (en) |
| HU (1) | HU182929B (en) |
| IL (1) | IL55546A (en) |
| IN (1) | IN149681B (en) |
| IT (1) | IT1098863B (en) |
| NZ (1) | NZ188438A (en) |
| PL (1) | PL107614B1 (en) |
| PT (1) | PT68556A (en) |
| SU (1) | SU1428175A3 (en) |
| ZA (1) | ZA785270B (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4512795A (en) * | 1982-01-16 | 1985-04-23 | Basf Aktiengesellschaft | Norbornane compounds, plant growth regulators containing these compounds, and their intermediates |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3001580A1 (en) * | 1980-01-17 | 1981-07-23 | Basf Ag, 6700 Ludwigshafen | METHOD FOR PRODUCING POLYCYCLIC NITROGEN-BASED COMPOUNDS |
| DE3124497A1 (en) * | 1981-06-23 | 1983-01-05 | Basf Ag, 6700 Ludwigshafen | METHOD FOR INFLUENCING PLANT GROWTH |
| DE69109057T2 (en) * | 1990-11-08 | 1995-09-21 | Ciba Geigy Ag | Pigment derivatives containing pyrazole. |
| WO1997010713A1 (en) * | 1995-09-21 | 1997-03-27 | Novartis Ag | 7-azabicyclo(4.2.0)oct-4-en-8-one derivates as plant-microbicides |
| GB0102907D0 (en) | 2001-02-06 | 2001-03-21 | Upf Uk Ltd | Vehicle door hinge |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3573281A (en) * | 1967-10-02 | 1971-03-30 | Huels Chemische Werke Ag | 2,10 - dioxa - 5 - aza-tricyclo(6,2,1,0**1,5) undecanedion-(6,9) and 2,11-dioxa-6-aza -tricyclo(7,2,1,0**1,6)dodecandedion-(7,10) compounds and their preparation |
| US3953444A (en) * | 1971-11-08 | 1976-04-27 | Syva Company | Cyclic and polycyclic diazadioxides as quenchers and radical inhibitors |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2615878C2 (en) * | 1976-04-10 | 1985-09-19 | Basf Ag, 6700 Ludwigshafen | Polycyclic nitrogenous compounds |
-
1977
- 1977-09-19 DE DE19772742034 patent/DE2742034A1/en not_active Withdrawn
-
1978
- 1978-09-11 IL IL55546A patent/IL55546A/en unknown
- 1978-09-11 IN IN993/CAL/78A patent/IN149681B/en unknown
- 1978-09-11 US US05/941,010 patent/US4259235A/en not_active Expired - Lifetime
- 1978-09-12 CA CA311,169A patent/CA1099259A/en not_active Expired
- 1978-09-13 AU AU39804/78A patent/AU519224B2/en not_active Expired
- 1978-09-14 PT PT68556A patent/PT68556A/en unknown
- 1978-09-14 DD DD78207823A patent/DD139201A5/en unknown
- 1978-09-15 EP EP78100908A patent/EP0001271B1/en not_active Expired
- 1978-09-15 DE DE7878100908T patent/DE2862069D1/en not_active Expired
- 1978-09-18 HU HU78BA3707A patent/HU182929B/en not_active IP Right Cessation
- 1978-09-18 PL PL1978209665A patent/PL107614B1/en unknown
- 1978-09-18 FI FI782848A patent/FI782848A/en unknown
- 1978-09-18 JP JP11370578A patent/JPS54117458A/en active Pending
- 1978-09-18 NZ NZ188438A patent/NZ188438A/en unknown
- 1978-09-18 ZA ZA00785270A patent/ZA785270B/en unknown
- 1978-09-18 CS CS786031A patent/CS200241B2/en unknown
- 1978-09-18 SU SU782665548A patent/SU1428175A3/en active
- 1978-09-18 DK DK411978A patent/DK411978A/en not_active Application Discontinuation
- 1978-09-18 BR BR7806112A patent/BR7806112A/en unknown
- 1978-09-18 AT AT673278A patent/AT359097B/en not_active IP Right Cessation
- 1978-09-19 IT IT27856/78A patent/IT1098863B/en active
-
1987
- 1987-01-16 JP JP62006293A patent/JPS62201871A/en active Granted
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3573281A (en) * | 1967-10-02 | 1971-03-30 | Huels Chemische Werke Ag | 2,10 - dioxa - 5 - aza-tricyclo(6,2,1,0**1,5) undecanedion-(6,9) and 2,11-dioxa-6-aza -tricyclo(7,2,1,0**1,6)dodecandedion-(7,10) compounds and their preparation |
| US3953444A (en) * | 1971-11-08 | 1976-04-27 | Syva Company | Cyclic and polycyclic diazadioxides as quenchers and radical inhibitors |
Non-Patent Citations (2)
| Title |
|---|
| Nelsen et al., J. Amer. Chem. Soc., vol. 96, pp. 1788 to 1793 (1974). * |
| Rieber et al., J. Amer. Chem. Soc., vol. 91, pp. 5668 and 5669 (1969). * |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4512795A (en) * | 1982-01-16 | 1985-04-23 | Basf Aktiengesellschaft | Norbornane compounds, plant growth regulators containing these compounds, and their intermediates |
Also Published As
| Publication number | Publication date |
|---|---|
| FI782848A (en) | 1979-03-20 |
| PT68556A (en) | 1978-10-01 |
| NZ188438A (en) | 1982-03-30 |
| ZA785270B (en) | 1979-09-26 |
| EP0001271A1 (en) | 1979-04-04 |
| PL107614B1 (en) | 1980-02-29 |
| AU519224B2 (en) | 1981-11-19 |
| IT7827856A0 (en) | 1978-09-19 |
| SU1428175A3 (en) | 1988-09-30 |
| DE2742034A1 (en) | 1979-03-29 |
| DE2862069D1 (en) | 1982-12-02 |
| PL209665A1 (en) | 1979-06-04 |
| DK411978A (en) | 1979-03-20 |
| BR7806112A (en) | 1979-05-08 |
| CS200241B2 (en) | 1980-08-29 |
| HU182929B (en) | 1984-03-28 |
| JPS54117458A (en) | 1979-09-12 |
| IN149681B (en) | 1982-03-13 |
| ATA673278A (en) | 1980-03-15 |
| JPS62201871A (en) | 1987-09-05 |
| AU3980478A (en) | 1980-03-20 |
| EP0001271B1 (en) | 1982-10-27 |
| IL55546A0 (en) | 1978-12-17 |
| AT359097B (en) | 1980-10-27 |
| JPH0558632B2 (en) | 1993-08-27 |
| CA1099259A (en) | 1981-04-14 |
| IT1098863B (en) | 1985-09-18 |
| IL55546A (en) | 1983-06-15 |
| DD139201A5 (en) | 1979-12-19 |
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